NCT Number: NCT00639366
Radiation Therapy to the Head in Preventing Brain Metastases in Women Receiving Trastuzumab and Chemotherapy for Metastatic or Locally Advanced Breast Cancer
RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. It is not yet known whether radiation therapy directed at the head is effective in preventing brain metastases in patients with advanced cancer.
PURPOSE: This randomized phase III trial is studying radiation therapy to the head to see how well it works in preventing brain metastases in women receiving trastuzumab and chemotherapy for metastatic or locally advanced breast cancer.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Phase 3
Primary location
Basildon University Hospital, Basildon, England, United Kingdom
About this study
OBJECTIVES:
- To test if prophylactic cranial radiotherapy delivering 30 Gy in 10 fractions will significantly reduce (from 35% to 21% at 2 years) the incidence of symptomatic brain metastases in patients treated with trastuzumab (Herceptin®) for metastatic breast cancer.
OUTLINE: This is a multicenter study. Patients are stratified by center, type of systemic therapy (trastuzumab [Herceptin®] monotherapy vs combination with chemotherapy), hormone receptor status, and presence of lung metastases (yes vs no). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive taxane/trastuzumab therapy for 6 weeks. While continuing taxane/trastuzumab therapy, patients then undergo 10 fractions of concurrent prophylactic cranial radiotherapy in the absence of disease progression or unacceptable toxicity.
- Arm II: Patients receive taxane/trastuzumab therapy without concurrent prophylactic cranial radiotherapy.
All patients undergo quality of life assessments every 8 weeks for 9 months.
After completion of study treatment, patients are followed periodically for at least 1 year.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Histologically proven breast carcinoma
- Metastatic or locally advanced disease
- Must demonstrate HER2 3+ positivity on IHC or 2+ over-expression and FISH test demonstrating C-erB2 gene amplification
- No known or suspected brain metastases or CNS disease, as defined by the presence of any of the following key symptoms:
- Headache
- Nausea and/or vomiting
- Clinical signs of raised intracranial pressure
- Seizures
- Focal symptoms
- Cognitive dysfunction
- Affective disorder
- Hormone receptor status not specified
PATIENT CHARACTERISTICS:
- Female
- Postmenopausal status not specified
- ECOG performance status 0 or 1
- Patients must a-priori be suitable for trastuzumab (Herceptin®) +/- chemotherapy in terms of bone marrow, hepatic, and renal function
- No prior history of cerebrovascular disease or neurological disorder including seizures
PRIOR CONCURRENT THERAPY:
- No prior cranial radiotherapy
- No prior neurosurgery
Treatment and study plan
Chemotherapy
Drugradiation therapy
RadiationPrimary outcomes
-
Incidence of symptomatic brain metastases
Secondary outcomes
-
Survival
-
Cerebral toxicity and quality of life
Sponsors and collaborators
Lead sponsor
Anglo Celtic Cooperative Oncology Group
Other
Registry information
Official study title
Prospective Randomised Clinical Trial Testing the Role of Prophylactic Cranial Radiotherapy in Patients Treated With Trastuzumab (Herceptin®) for Metastatic Breast Cancer
Important dates
- Study start
- 2007
- Primary completion
- 2010
- Study completion
- 2010
- First posted
- Mar 20, 2008
- Registry last updated
- Aug 7, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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